Skip Nav Destination
Close Modal
Search Results for
qmpsf-quantitative-multiplex-pcr-short-fluorescent-fragments
Update search
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
NARROW
Format
Journal
Article Type
Topics
Issue Section
Date
Availability
1-1 of 1 Search Results for
qmpsf-quantitative-multiplex-pcr-short-fluorescent-fragments
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Sort by
Journal Articles
Christine Bellanné-Chantelot, Séverine Clauin, Dominique Chauveau, Philippe Collin, Michèle Daumont, Claire Douillard, Danièle Dubois-Laforgue, Laurent Dusselier, Jean-François Gautier, Michel Jadoul, Marie Laloi-Michelin, Laetitia Jacquesson, Etienne Larger, Jacques Louis, Marc Nicolino, Jean-François Subra, Jean-Marie Wilhem, Jacques Young, Gilberto Velho, José Timsit
Journal:
Diabetes
Diabetes 2005;54(11):3126–3132
Published: 01 November 2005
... by sequencing. Patients without mutations were then screened for TCF2 rearrangements by the quantitative multiplex PCR of short fluorescent fragments (QMPSF). Among the 40 patients, the overall detection rate was 70%: 18 had point mutations, 9 had whole-gene deletions, and 1 had a deletion of a single...
Includes: Supplementary data